FDA UDI In Commercial Distribution 🇺🇸 United States

GLOBAL APG+

DI: 10603295104759 · Model: 2230-10-030 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GLOBAL APG+
Primary DI
10603295104759
Version / Model
2230-10-030
Catalog Number
223010030
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
c0a12f86-5180-4611-9d8d-ae76e64b9d3d

Device Description

GLOBAL APG+ LOW PROFILE CENTRAL REAMER SIZE 40/44 RU

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWR DRIVER, PROSTHESIS

GMDN Terms

Code Name
45115 Medullary canal orthopaedic reamer, rigid

Identifiers

Type ID
Primary 10603295104759

Customer Contacts